19503742

Source:http://linkedlifedata.com/resource/pubmed/id/19503742

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0042170, umls-concept:C0220825, umls-concept:C1419102, umls-concept:C1556094, umls-concept:C1882417
pubmed:dateCreated	2009-6-8
pubmed:abstractText	Vogt-Koyanagi-Harada (VKH) disease is an autoimmune disorder against melanocytes. Polymorphisms of the protein tyrosine phosphatase non-receptor 22 gene (PTPN22) have recently been reported to be associated with susceptibility to several autoimmune diseases. In this study, genetic susceptibility to VKH disease was investigated by screening for single nucleotide polymorphisms (SNPs) of PTPN22.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-11120868, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-11169242, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-11336942, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-11752280, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-11791212, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-12436197, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-147420, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15004560, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15208781, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15229958, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15273934, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15565104, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15670805, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15719322, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-15953440, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-16052563, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-16314859, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-16690758, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-17200659, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-17237219, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-17295139, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-18199975, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-18282809, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-18578611, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-19122825, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-19234630, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-7725227, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-7908535, http://linkedlifedata.com/resource/pubmed/commentcorrection/19503742-7928186
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/PTPN22 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatase...
pubmed:status	MEDLINE
pubmed:issn	1090-0535
pubmed:author	pubmed-author:AsukataYuriY, pubmed-author:HorieYukihiroY, pubmed-author:InokoHidetoshiH, pubmed-author:IshidaSusumuS, pubmed-author:KatsuyamaYoshihikoY, pubmed-author:KitaichiNobuyoshiN, pubmed-author:MarksP GPG, pubmed-author:MiuraToshieT, pubmed-author:MizukiNobuhisaN, pubmed-author:OhnoShigeakiS, pubmed-author:YoshidaKazuhikoK
pubmed:issnType	Electronic
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1115-9
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:19503742-Chi-Square Distribution, pubmed-meshheading:19503742-Female, pubmed-meshheading:19503742-Gene Frequency, pubmed-meshheading:19503742-Humans, pubmed-meshheading:19503742-Japan, pubmed-meshheading:19503742-Linkage Disequilibrium, pubmed-meshheading:19503742-Male, pubmed-meshheading:19503742-Polymorphism, Single Nucleotide, pubmed-meshheading:19503742-Protein Tyrosine Phosphatase, Non-Receptor Type 22, pubmed-meshheading:19503742-Sequence Analysis, DNA, pubmed-meshheading:19503742-Uveomeningoencephalitic Syndrome
pubmed:year	2009
pubmed:articleTitle	Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
pubmed:affiliation	Department of Ophthalmology, Hokkaido University Graduate School of Medicine, Kita-ku, Sapporo, Japan. y-horie@med.hokudai.ac.jp
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't